[HTML][HTML] Shikonin inhibits tumor growth in mice by suppressing pyruvate kinase M2-mediated aerobic glycolysis

X Zhao, Y Zhu, J Hu, L Jiang, L Li, S Jia, K Zen - Scientific reports, 2018 - nature.com
X Zhao, Y Zhu, J Hu, L Jiang, L Li, S Jia, K Zen
Scientific reports, 2018nature.com
Shift metabolism profile from mitochondrial oxidative phosphorylation to aerobic glycolysis
(Warburg effect) is a key for tumor cell growth and metastasis. Therefore, suppressing the
tumor aerobic glycolysis shows a great promise in anti-tumor therapy. In the present study,
we study the role of shikonin, a naphthoquinone isolated from the traditional Chinese
medicine Lithospermum, in inhibiting tumor aerobic glycolysis and thus tumor growth. We
found that shikonin dose-dependently inhibited glucose uptake and lactate production in …
Abstract
Shift metabolism profile from mitochondrial oxidative phosphorylation to aerobic glycolysis (Warburg effect) is a key for tumor cell growth and metastasis. Therefore, suppressing the tumor aerobic glycolysis shows a great promise in anti-tumor therapy. In the present study, we study the role of shikonin, a naphthoquinone isolated from the traditional Chinese medicine Lithospermum, in inhibiting tumor aerobic glycolysis and thus tumor growth. We found that shikonin dose-dependently inhibited glucose uptake and lactate production in Lewis lung carcinoma (LLC) and B16 melanoma cells, confirming the inhibitory effect of shikonin on tumor aerobic glycolysis. Treatment of shikonin also decreased tumor cell ATP production. Furthermore, pyruvate kinase M2 (PKM2) inhibitor or activator respectively altered the effect of shikonin on tumor cell aerobic glycolysis, suggesting that suppression of cell aerobic glycolysis by shikonin is through decreasing PKM2 activity. Western blot analysis confirmed that shikonin treatment reduced tumor cell PKM2 phosphorylation though did not reduce total cellular PKM2 level. In vitro assay also showed that shikonin treatment significantly promoted tumor cell apoptosis compared to untreated control cells. Finally, when mice implanted with B16 cells were administered with shikonin or control vehicle, only shikonin treatment significantly decreased B16 tumor cell growth. In conclusion, this study demonstrates that shikonin inhibits tumor growth in mice by suppressing PKM2-mediated aerobic glycolysis.
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